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FDA 510(k) Applications Submitted by Double Medical Technology Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K220921
03/30/2022
Metal Bone Screw
Double Medical Technology Inc.
K221088
04/13/2022
Anatomic Bone Plate
Double Medical Technology Inc.
K221090
04/13/2022
Metal Cannulated Screw
Double Medical Technology Inc.
K221150
04/20/2022
Advanced Bone Plate
Double Medical Technology Inc.
K221221
04/27/2022
Advanced Intramedullary Nail System
Double Medical Technology Inc.
K172830
09/18/2017
Double Medical Femoral Nail System
Double Medical Technology Inc.
K223753
12/14/2022
Cervical Plate System
Double Medical Technology Inc.
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